Chromosomal instability by low-coverage whole-genome sequencing assay predicts prognosis in bladder cancer patients underwent radical cystectomy.

IF 2.1 4区 医学 Q3 GENETICS & HEREDITY
Qi Ding, Hailiang Zhu, Bo Fan, Lisheng Wang, Xiaohua Jin, Cheng Cao, Ying Shi, Zhijiang Fan, Wenjian Tu, Feng Li
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引用次数: 0

Abstract

Purpose: To investigate chromosomal instability (CIN) in tumor tissue from radical bladder resection and to evaluate whether it can be used as a biomarker for the molecular typing of (BC).

Methods: DNA was extracted from formalin-fixed paraffin-embedded samples of 50 BC patients who were followed up to March 23 2023 using the Qiagen nucleic acid kits. We analyzed CIN in tumor of bladder by low-coverage whole genome sequencing (LC-WGS). Kaplan-Meier log-rank test was used to perform survival analysis. The association between variables and overall and progression-free survival was analyzed using the Cox proportional hazards model.

Results: There were 44 genome segments with statistically significant changes in copy number. CIN was significantly correlated with tumor stage, lymph node metastasis, relapse and survival status. Patients with high CIN were found to have a worse survival, with a median overall survival (OS) of 15 months. In addition, patients with high CIN were more likely to relapse, with a median progression-free survival (PFS) of 7 months. Patients with low CIN showed better OS and PFS. However, there was no significant difference in OS and PFS between T2 and T3-T4 patients. Multivariate cox regression analysis showed that high CIN was an independent predictor of OS, and high CIN and muscle invasion were independent predictors of PFS. Furthermore, patients with abnormal copy number of a single chromosome also had a poor prognosis, with a median survival of 14-30 months for OS and 5-10 months for PFS, while negative patients had a better prognosis.

Conclusion: CIN was significantly correlated with tumor stage, lymph node metastasis, relapse and survival status of BC. Patients with high CIN or abnormal copy numbers of a single chromosome have a poor prognosis. CIN might be better than T stage in predicting the prognosis of patients with BC. Molecular typing of CIN can be used as an independent prognostic factor for BC.

用低覆盖率全基因组测序法预测膀胱癌根治性膀胱切除术患者的预后。
目的:研究膀胱癌根治术后肿瘤组织的染色体不稳定性(CIN),并评价其是否可作为膀胱癌分子分型的生物标志物。方法:采用Qiagen核酸试剂盒对50例BC患者进行福尔马林固定石蜡包埋标本提取DNA,随访至2023年3月23日。我们采用低覆盖全基因组测序(LC-WGS)分析膀胱肿瘤中CIN的表达。采用Kaplan-Meier log-rank检验进行生存分析。使用Cox比例风险模型分析变量与总生存率和无进展生存率之间的关系。结果:共有44个基因组片段拷贝数变化有统计学意义。CIN与肿瘤分期、淋巴结转移、复发及生存状态有显著相关性。高CIN患者的生存期较差,中位总生存期(OS)为15个月。此外,CIN高的患者更容易复发,中位无进展生存期(PFS)为7个月。低CIN患者有较好的OS和PFS。然而,T2和T3-T4患者的OS和PFS无显著差异。多因素cox回归分析显示,高CIN是OS的独立预测因子,高CIN和肌肉侵袭是PFS的独立预测因子。此外,单染色体拷贝数异常的患者预后也较差,OS中位生存期为14-30个月,PFS中位生存期为5-10个月,阴性患者预后较好。结论:CIN与BC的肿瘤分期、淋巴结转移、复发及生存状况有显著相关性。CIN高或单染色体拷贝数异常的患者预后较差。CIN在预测BC患者预后方面可能优于T期。CIN的分子分型可作为BC的独立预后因素。
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来源期刊
BMC Medical Genomics
BMC Medical Genomics 医学-遗传学
CiteScore
3.90
自引率
0.00%
发文量
243
审稿时长
3.5 months
期刊介绍: BMC Medical Genomics is an open access journal publishing original peer-reviewed research articles in all aspects of functional genomics, genome structure, genome-scale population genetics, epigenomics, proteomics, systems analysis, and pharmacogenomics in relation to human health and disease.
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